CA1175307A - Metallised labels - Google Patents
Metallised labelsInfo
- Publication number
- CA1175307A CA1175307A CA000381815A CA381815A CA1175307A CA 1175307 A CA1175307 A CA 1175307A CA 000381815 A CA000381815 A CA 000381815A CA 381815 A CA381815 A CA 381815A CA 1175307 A CA1175307 A CA 1175307A
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- lacquer
- parts
- label
- solution
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Abstract
A B S T R A C T
The present invention relates to indirectly metallized labels for containers, such as bottles, coated with a lacquer that has been applied before metallizing, comprising 2 to 10 weight % (calculated on the amount of resin of said lacquer) of additives, which do not attack the metal of said labels and which are soluble in an aqueous caustic soda solution, containing 1.5 weight % of caustic soda, having a temperature of 80°C.
The present invention relates to indirectly metallized labels for containers, such as bottles, coated with a lacquer that has been applied before metallizing, comprising 2 to 10 weight % (calculated on the amount of resin of said lacquer) of additives, which do not attack the metal of said labels and which are soluble in an aqueous caustic soda solution, containing 1.5 weight % of caustic soda, having a temperature of 80°C.
Description
1 ~7530~
Metallised labels The present invention relates to metallised labels for containers such as bottles.
It is known that in the labelling industry there is a requirement for labels having a metallic appearance. It is obvious to use for this purpose a metallic foil. However, with respect to returnable bottles, such labels cannot be removed by using standard techni~ues, involving immersion in a bath of 1.5 weight % of caustic soda, having a temperature of ~0C, within a period of 3 minutes. Further in such a bath metallic foil labels react with caustic soda, due to which its strength is reduced such that the caustic soda has to be changed frequently.
For said reasons, it would be advantageous to use metallised papers for this purpose, since such papers have a low metal content in comparison with a metallic foil.
Metallised papers are generally known. A very useful type is disclosed in Dutch Patent application 8,000,967 (in the name of the assignee of the present application and published September 16, 1981) as with a foil label the requirements are ~0 the same of which the chief are appearance and ease of removal in the above caustic soda solution. Lacquersj preferably acrylic resin based lacquers, are used to provide protection for the metallic layer against water and oxygen and also to enable the product to perform satisfactorily on labelling machines.
In order to enable a metallised label to be satisfactorily removed from a bottle, it is necessary that the hot caustic soda solution can attack the adhesive layer between ~bottle and paper. For this to occur within a relatively short time, the caustic soda has to rapidly reach the paper layer.
That is to say it must rapidly pass through the lacquer and metallised layer. The latter problem is obvlated with this invention in that a very thin layer of metal which has been vacuum deposited in the label construction will provide a low resistance to the hot dilute caustic soda solution.
There are two potential ways of achieving the desired penetration of the lacquer.
1 1~530~
, solubility of lacquer - thickness of lacquer The commercially available lacquers which are readily dissolved by dilute alkali are ideally suited for applications involving direc-t metallising where the lacquer is applied after metallising. ~lowever, the resultant products from direc-t metallising have an inferior mirror reflec-tivity as compared with indireet metallised papers.
Such lac~uers, whieh are used for diree-t metallised labels are not suitable in the indireet process where the lacquer is applied before metallising because the lacquer must have low volatiles at reduced pressures.
Laequers soluble in dilute alkali and having low volatiles under redueed pressure are not eommereially available.
It would be possible to employ a thin laequer layer thereby allowing the eaustie soda to reaeh the metallised layer by a permeation mechanism. This has appeared to be unsatisfaetory. If the laequer thiekness is less than about 1.7 um, interferenee fringes may oeeur whieh detraet from the end produet's appearanee.
It was found now, that metallised labels, glued to bottles by means o~ a glue that is not resistant against an aqueous eaustic soda -solution, containing 1.5 % by weight of caustic soda, at a temperature of 80 C, may be removed within a period of 3 minutes from said bottles, by using labels coated with a laequer wherein 2 to 10 weight % hot ; dilute alkali soluble additives that do not attaek the metal Iayer of said label have been ineorporated. When said additives have been dissoIved ln said allcaline solution, thé laequer eoating starts -to eraek or to split and to swell. Subsequently the underlying metallic layè~r~ls;dissolved`and -Finally the paper subs-trate and glue (easein based) are attacked. Sueh additives may be dissolvecl and subsequently dispersed or directly ground into -the lacquer. The preferred laequers and -techniques of manufacture are those used in DPA 80.00967.
Preferably said additives are distribu-ted in said lacquer a-t a particle size of up to 2 um.
Further it is preferrecl-that said additives are Food and Drug Act (F.D.A.) approved.
Evidently it is preferred that said adclitives do not react with caustic soda and have a low vapor prcssure.
~ .
`" 11?~3~ ~
In many cases it is preferred that said additives are colourless or clear.
Preferred additives are sugar-like materials such as sucrose, mannitol and urea. Also water based resins 9 including acrylic emulsions, polyvinylalcohols and polyacrylamides, substituted celluloses, such as nitrocellulose, carboxyethyl and carboxymethyl cellulosesand urea-formaldehyde types (e.g. melamine) may similarly be included.
Further it is preferred that a paper is used which has been subJected to steam or conditioned at high humidity immediately prior to the laminating step described in DPA 60.00967. The resultant label has been found to give beneficial results with respect~-to processing at the printing and label application stages and with respect to ease of label removal from the container.
The mirror reflectivity of a sample surface can be measured by adherring a 150 mm x 200 mm sample to a smooth flat glass surface. At an angle of 60 to the sample is placed a 150 mm x 250 mm grid on which is marked 10 mm squares and numerals 1-25 in the vertical direction.
The sample surface is illuminated by standard photographic lamps A 5" x 4l1 Micro Precision Products Technical Camara with a Schneider Xenar 1:4.5/150 lens and aperture F16 is situated 500 mm from the point of contact of grid and sample~at an angle of 30 to sample-. The focus is on the reflected numeral 1 from the grid and a photograph is taken. The mirror reflectivity of the sample surface is determined by examination of the photograph to see the highest number at which a clear reflected image is obtained. This number gives the mirror reflectivity rating of the sample surface.
Example 1 A lacquer solution was prepared by dis~olving 100 parts by weight of Bakelite*Vinyl Solution Resin VMCH in 300 parts by weight of butanone-2. The resultant lacquer solution was applied to the ca~rier film at a dry coating weight of 2.2 grams per square meter (gsm) using a drying temperature of 7~C.
A coherent continuous stratum of aluminium metal was then vapour deposited by standard methods upon this lacquer layer.
A layer of solvent based laminating adhesive Adcote ~40 was applied to the metal layer at a dry coating weight of 2.~ gsm to bond the carrier (Hescolina Base paper (60 gsm)) to the composite.
*Trade mark ~ ~!
117~307 r After 7 days the carrier film was stripped from the composite structure to produce a laminar product which had a reflectivity rating of 5, according to the method described in the text.
From the resultant laminar product was cut a 100 mmx 100 mm label which was bonded to a glass bottle using a standard casein glue (ex Houstr~). After 7 days storage at ambient conditions the bottle plus label was immersed in a 1.5 % aqueous caustic soda solution at The label failed to release after 25 minutes.
Example 2 3.0 parts by weight of sucrose were dissolved in~-9 parts of water and this solution was mixed into a lacquer solution comprising 100 parts by weight of Bakelite Vinyl Solution Resin VMCH, 300 parts by weight of butanone-2, The resultant lacquer solution was applied to a polypropylene carrier film at a dry coating weight of 2.4 gsm using a drying temperature of 70C.
A coherent continuous stratum of aluminium metal was then vapour deposited by standard methods upon this lacquer layer.
7.5 parts by weight of sucrose were dissolved in 22.5 parts of water and this was mixed into a laminating adhesive solution comprising 100 parts of- Adcote 340, 115 parts by weight of methanol and 15 parts of catalyst. The resultant laminating adhesive solution was applied to the metal layer at a dry coating weight of 30 gsm to bond the Hescolina Base Paper (60 gsm) to the composite.
After 7 days the carrier film was stripped from the composite structure to produce a laminar product which had a mirror reflectivity rating of 4~ determined according to the method described in the text.
From the resultant laminar product was cut a 100 mm x 100 mm label which was bonded to a glass bottle using a standard casein glue (ex Houstra). After 7 days storage at ambient conditions the bottle - plus label was immersed in a 1.5 ~ aqueous caustic soda solution at The label released from the bottle after 7 minutesO
*Trade mar~
~ .
~ 117~307 r A lacquer solution was prepared by dissolving 70 parts by weight of Neocryl*~811 (ex Polyvinyl Chemie) and 30 parts by weight of Vinnol*
H40/55 (ex Wacker) in 210 parts by weight of butanone-2 and 90 parts by weight of ethyl acetate.
The resultant lacquer was applied to the polyester carrier film at a dry coating weight of 2.5 gsm using a drying temperature of 70C.
A coherent continuous stratum of aluminium metal was then vapour deposited by standard methods upon this lacquer surface.
A layer of an aqueous based styrene butadiene emulsion adhesive was applied to the metal layer at a dry coating weight of 4 gsm to bond the substrate (Hescolina*base paper (60 gsm)) to the composite.
After 7 days the carrier film was stripped from the composite structure to produce a laminar product with a mirror reflectivity of 5. From the resultant laminar product was cut a lOO,mm x 100 mm label which was bonded to a glass bottle using a standard casein glue.
After 7 days storage at ambient conditions, the bottle plus label was immersed in a 1.5 % caustic soda solution at 80C.
The label released from the bottle after 14 minutes.
ExampIe 4 As example 3 but 3 parts by weight of sucrose dissolved in 9 parts by weight of water were added to the lacquer.
Mirror reflectivity rating of 4.
~ The label removal time was 3.5 minutes.
Example 5 As example 3 but 3 parts by weight of sucrose were ground into the lacquer.
Mirror reflectivity rating of 5.
The label removal time was 158 seconds.
Example 6 As example 3 but 5 parts by weight of dextrose monohydrate were ground into the lacquerO
Mirror reflectivity rating of 4.
-The label removal time was 130 seconds.
- . -I
*Trade mark 1~
r ~ 3 0 ~
Example 7 As example 3 but 7 parts by weight o-f sucrose were ground into thc lacquer.
I~lirror reflectivity rating of 4.
The label removal time was 220 seconds.
Example 8 A lacquer solution was prepared by dissolving 75 parts by weight of lleocryl B 811 and 25 parts by weight of Vinnol H 40/55 in 210 parts by weight o-f butanone-2 and 90 parts by weight o-f ethyl acetate.
To this solution were added 3 parts by weight of sucrose dissolved in 9 parts by weight of water. The resultant lacquer solut-ion was applied to the polyester carrier film at a dry coa-ting weight of 2.6 gsm using a drying temperature of 70C.
Then as example 3.
Mirror reflectivity 4.
The label released from the bottle after lOS seconds.
Example 9 As example 8 but 5 parts by weight of sucrose were ground into the lacquer.
Mirror reflectivity 4. ---The label released from the bottle after 95 seconds.
Example 10 A lacquer solution was prepared by dissolving 80 parts by weight of~ileocryl B 811 and 20 parts by weight of Vinnol H 40/SS in 210 parts by weight of butanone-2 and 90 parts by weight of ethyl ace-tate.
To this solution were added 5 parts by weight of sucrose dissolved in~15 parts by weight o~ water. The resultan-t lacquer solution ~vas applied to the polyester carrier film at a dry coating weight of 2.6 gsm~using a~drying temperature of 70C.
30~ Then as example 3.
llirror reflectivity 4.
The label released from the bottle after 115 seconds.
Example: 11 As example 10 but 5 parts by weight of sucrose were ground into thc lacquer.
llirror re-Flectivity 5.
The label removal time was 9G seconds.
, .
~ ~753~ `
Example 12 A lacquer solution was prepared by dissolving 80 parts by weight of Neocryl B 811 and 20 parts by weight of Vinnol H 40/55 in 210 parts by weight of butanone-2 and 90 parts by weight of ethyl acetate. To this solution was added 10 parts by weight of Neocryl BT21 (ex Poly-vinyl Chemie) which is an emulsion in water. The resultant lacquer solution was applied to a polyester carrier film at a dry coating weight of 1.7 gsm using a drying temperature of ROC, A coherent continuous stratum of aluminum metal was then vapour deposited by standard methods upon this lacquer surface.
A layer of an aqueous based styrene butadiene adhesive was applied to the metal layer at a dry coating weight of 4 gsm to bond the substrate (Hescolina base paper 60 gsm which had been subJected to steam at 20 psi for 10 seconds) to the composite.
After 7 days the carrier film was stripped from the composite structure to produce a laminar product.
Th~n as example 3.
Mirror reflectivity 4.
The label removal time was 150 seconds.
Example 13 A lacquer solution was prepared by dissolving 80 parts by weight of Neocryl B 811 and 20 parts by weight of VinnoI H 40/55 in 210 parts by weight of butanone-2 and 90 parts by weight of ethyl acetate. To this solution was added 5 parts by weight of polyvinylàlcohol Poval *
105 ex Kuraray* dissolved in 25 parts of water.
The resultant lacquer solution was applied to a polyester carrier film at a dry coating weight of 1.7 gsm using a drying temperature of 80C.
A coherent continuous stratum of aluminum metal was then vapour deposited by standard methods upon this lacquer surface.
A layer of an aqueous based styrene butadiene adhesive was applied to the metaI layer at a dry coating weight of 4 gsm to bond the substrate (~lescoline base paper 60 gsm which had been subJected to steam at 20 psi for 10 seconds) to the composite.
After 7 days the carrier film was stripped from the composite structure to produce a laminar product.
.
~ *Trade mark .
~17~307 Then as example 3.
The resultant laminar product had a mirror reflectivity of 5 and the label released from the bottle after 160 seconds.
Example 14 A lacquer solution was prepared by dissolving 80 parts by weight of Neocryl B 811 and ~0 parts by weight of Vinnol H 40/55 in 210 parts by weight-of butanone-2 and 90 par-ts by weight of ethyl acetate. To this solution was added 10 parts by weight of Neocryl BT21 ~ex Polyvinyl Chemie) which is an emulsion in water.
The resultant lacquer solution was applied to a polyester carrier film at a dry coating weight of 1.7 gsm using ~ drying temperature of 80C.
A coherent con-tinuous stratum of aluminum metal was then vapour deposited by standard me-thods upon this la_quer surface.
A layer of an aqueous based styrene butadiene adhesive was applied to the metal layer at a dry coa-ting weight of 4 gsm to bond the substrate (Hescolina base paper 60 gsm, that had not been subJected to a steam treatment) to the composite.
After 7 days the carrier film was stripped from the composite structure to produce a laminar product~
The as example 3.
The product had a reflectivity of 6 and the label released from the bottle after 160 seconds.
:~
:
Metallised labels The present invention relates to metallised labels for containers such as bottles.
It is known that in the labelling industry there is a requirement for labels having a metallic appearance. It is obvious to use for this purpose a metallic foil. However, with respect to returnable bottles, such labels cannot be removed by using standard techni~ues, involving immersion in a bath of 1.5 weight % of caustic soda, having a temperature of ~0C, within a period of 3 minutes. Further in such a bath metallic foil labels react with caustic soda, due to which its strength is reduced such that the caustic soda has to be changed frequently.
For said reasons, it would be advantageous to use metallised papers for this purpose, since such papers have a low metal content in comparison with a metallic foil.
Metallised papers are generally known. A very useful type is disclosed in Dutch Patent application 8,000,967 (in the name of the assignee of the present application and published September 16, 1981) as with a foil label the requirements are ~0 the same of which the chief are appearance and ease of removal in the above caustic soda solution. Lacquersj preferably acrylic resin based lacquers, are used to provide protection for the metallic layer against water and oxygen and also to enable the product to perform satisfactorily on labelling machines.
In order to enable a metallised label to be satisfactorily removed from a bottle, it is necessary that the hot caustic soda solution can attack the adhesive layer between ~bottle and paper. For this to occur within a relatively short time, the caustic soda has to rapidly reach the paper layer.
That is to say it must rapidly pass through the lacquer and metallised layer. The latter problem is obvlated with this invention in that a very thin layer of metal which has been vacuum deposited in the label construction will provide a low resistance to the hot dilute caustic soda solution.
There are two potential ways of achieving the desired penetration of the lacquer.
1 1~530~
, solubility of lacquer - thickness of lacquer The commercially available lacquers which are readily dissolved by dilute alkali are ideally suited for applications involving direc-t metallising where the lacquer is applied after metallising. ~lowever, the resultant products from direc-t metallising have an inferior mirror reflec-tivity as compared with indireet metallised papers.
Such lac~uers, whieh are used for diree-t metallised labels are not suitable in the indireet process where the lacquer is applied before metallising because the lacquer must have low volatiles at reduced pressures.
Laequers soluble in dilute alkali and having low volatiles under redueed pressure are not eommereially available.
It would be possible to employ a thin laequer layer thereby allowing the eaustie soda to reaeh the metallised layer by a permeation mechanism. This has appeared to be unsatisfaetory. If the laequer thiekness is less than about 1.7 um, interferenee fringes may oeeur whieh detraet from the end produet's appearanee.
It was found now, that metallised labels, glued to bottles by means o~ a glue that is not resistant against an aqueous eaustic soda -solution, containing 1.5 % by weight of caustic soda, at a temperature of 80 C, may be removed within a period of 3 minutes from said bottles, by using labels coated with a laequer wherein 2 to 10 weight % hot ; dilute alkali soluble additives that do not attaek the metal Iayer of said label have been ineorporated. When said additives have been dissoIved ln said allcaline solution, thé laequer eoating starts -to eraek or to split and to swell. Subsequently the underlying metallic layè~r~ls;dissolved`and -Finally the paper subs-trate and glue (easein based) are attacked. Sueh additives may be dissolvecl and subsequently dispersed or directly ground into -the lacquer. The preferred laequers and -techniques of manufacture are those used in DPA 80.00967.
Preferably said additives are distribu-ted in said lacquer a-t a particle size of up to 2 um.
Further it is preferrecl-that said additives are Food and Drug Act (F.D.A.) approved.
Evidently it is preferred that said adclitives do not react with caustic soda and have a low vapor prcssure.
~ .
`" 11?~3~ ~
In many cases it is preferred that said additives are colourless or clear.
Preferred additives are sugar-like materials such as sucrose, mannitol and urea. Also water based resins 9 including acrylic emulsions, polyvinylalcohols and polyacrylamides, substituted celluloses, such as nitrocellulose, carboxyethyl and carboxymethyl cellulosesand urea-formaldehyde types (e.g. melamine) may similarly be included.
Further it is preferred that a paper is used which has been subJected to steam or conditioned at high humidity immediately prior to the laminating step described in DPA 60.00967. The resultant label has been found to give beneficial results with respect~-to processing at the printing and label application stages and with respect to ease of label removal from the container.
The mirror reflectivity of a sample surface can be measured by adherring a 150 mm x 200 mm sample to a smooth flat glass surface. At an angle of 60 to the sample is placed a 150 mm x 250 mm grid on which is marked 10 mm squares and numerals 1-25 in the vertical direction.
The sample surface is illuminated by standard photographic lamps A 5" x 4l1 Micro Precision Products Technical Camara with a Schneider Xenar 1:4.5/150 lens and aperture F16 is situated 500 mm from the point of contact of grid and sample~at an angle of 30 to sample-. The focus is on the reflected numeral 1 from the grid and a photograph is taken. The mirror reflectivity of the sample surface is determined by examination of the photograph to see the highest number at which a clear reflected image is obtained. This number gives the mirror reflectivity rating of the sample surface.
Example 1 A lacquer solution was prepared by dis~olving 100 parts by weight of Bakelite*Vinyl Solution Resin VMCH in 300 parts by weight of butanone-2. The resultant lacquer solution was applied to the ca~rier film at a dry coating weight of 2.2 grams per square meter (gsm) using a drying temperature of 7~C.
A coherent continuous stratum of aluminium metal was then vapour deposited by standard methods upon this lacquer layer.
A layer of solvent based laminating adhesive Adcote ~40 was applied to the metal layer at a dry coating weight of 2.~ gsm to bond the carrier (Hescolina Base paper (60 gsm)) to the composite.
*Trade mark ~ ~!
117~307 r After 7 days the carrier film was stripped from the composite structure to produce a laminar product which had a reflectivity rating of 5, according to the method described in the text.
From the resultant laminar product was cut a 100 mmx 100 mm label which was bonded to a glass bottle using a standard casein glue (ex Houstr~). After 7 days storage at ambient conditions the bottle plus label was immersed in a 1.5 % aqueous caustic soda solution at The label failed to release after 25 minutes.
Example 2 3.0 parts by weight of sucrose were dissolved in~-9 parts of water and this solution was mixed into a lacquer solution comprising 100 parts by weight of Bakelite Vinyl Solution Resin VMCH, 300 parts by weight of butanone-2, The resultant lacquer solution was applied to a polypropylene carrier film at a dry coating weight of 2.4 gsm using a drying temperature of 70C.
A coherent continuous stratum of aluminium metal was then vapour deposited by standard methods upon this lacquer layer.
7.5 parts by weight of sucrose were dissolved in 22.5 parts of water and this was mixed into a laminating adhesive solution comprising 100 parts of- Adcote 340, 115 parts by weight of methanol and 15 parts of catalyst. The resultant laminating adhesive solution was applied to the metal layer at a dry coating weight of 30 gsm to bond the Hescolina Base Paper (60 gsm) to the composite.
After 7 days the carrier film was stripped from the composite structure to produce a laminar product which had a mirror reflectivity rating of 4~ determined according to the method described in the text.
From the resultant laminar product was cut a 100 mm x 100 mm label which was bonded to a glass bottle using a standard casein glue (ex Houstra). After 7 days storage at ambient conditions the bottle - plus label was immersed in a 1.5 ~ aqueous caustic soda solution at The label released from the bottle after 7 minutesO
*Trade mar~
~ .
~ 117~307 r A lacquer solution was prepared by dissolving 70 parts by weight of Neocryl*~811 (ex Polyvinyl Chemie) and 30 parts by weight of Vinnol*
H40/55 (ex Wacker) in 210 parts by weight of butanone-2 and 90 parts by weight of ethyl acetate.
The resultant lacquer was applied to the polyester carrier film at a dry coating weight of 2.5 gsm using a drying temperature of 70C.
A coherent continuous stratum of aluminium metal was then vapour deposited by standard methods upon this lacquer surface.
A layer of an aqueous based styrene butadiene emulsion adhesive was applied to the metal layer at a dry coating weight of 4 gsm to bond the substrate (Hescolina*base paper (60 gsm)) to the composite.
After 7 days the carrier film was stripped from the composite structure to produce a laminar product with a mirror reflectivity of 5. From the resultant laminar product was cut a lOO,mm x 100 mm label which was bonded to a glass bottle using a standard casein glue.
After 7 days storage at ambient conditions, the bottle plus label was immersed in a 1.5 % caustic soda solution at 80C.
The label released from the bottle after 14 minutes.
ExampIe 4 As example 3 but 3 parts by weight of sucrose dissolved in 9 parts by weight of water were added to the lacquer.
Mirror reflectivity rating of 4.
~ The label removal time was 3.5 minutes.
Example 5 As example 3 but 3 parts by weight of sucrose were ground into the lacquer.
Mirror reflectivity rating of 5.
The label removal time was 158 seconds.
Example 6 As example 3 but 5 parts by weight of dextrose monohydrate were ground into the lacquerO
Mirror reflectivity rating of 4.
-The label removal time was 130 seconds.
- . -I
*Trade mark 1~
r ~ 3 0 ~
Example 7 As example 3 but 7 parts by weight o-f sucrose were ground into thc lacquer.
I~lirror reflectivity rating of 4.
The label removal time was 220 seconds.
Example 8 A lacquer solution was prepared by dissolving 75 parts by weight of lleocryl B 811 and 25 parts by weight of Vinnol H 40/55 in 210 parts by weight o-f butanone-2 and 90 parts by weight o-f ethyl acetate.
To this solution were added 3 parts by weight of sucrose dissolved in 9 parts by weight of water. The resultant lacquer solut-ion was applied to the polyester carrier film at a dry coa-ting weight of 2.6 gsm using a drying temperature of 70C.
Then as example 3.
Mirror reflectivity 4.
The label released from the bottle after lOS seconds.
Example 9 As example 8 but 5 parts by weight of sucrose were ground into the lacquer.
Mirror reflectivity 4. ---The label released from the bottle after 95 seconds.
Example 10 A lacquer solution was prepared by dissolving 80 parts by weight of~ileocryl B 811 and 20 parts by weight of Vinnol H 40/SS in 210 parts by weight of butanone-2 and 90 parts by weight of ethyl ace-tate.
To this solution were added 5 parts by weight of sucrose dissolved in~15 parts by weight o~ water. The resultan-t lacquer solution ~vas applied to the polyester carrier film at a dry coating weight of 2.6 gsm~using a~drying temperature of 70C.
30~ Then as example 3.
llirror reflectivity 4.
The label released from the bottle after 115 seconds.
Example: 11 As example 10 but 5 parts by weight of sucrose were ground into thc lacquer.
llirror re-Flectivity 5.
The label removal time was 9G seconds.
, .
~ ~753~ `
Example 12 A lacquer solution was prepared by dissolving 80 parts by weight of Neocryl B 811 and 20 parts by weight of Vinnol H 40/55 in 210 parts by weight of butanone-2 and 90 parts by weight of ethyl acetate. To this solution was added 10 parts by weight of Neocryl BT21 (ex Poly-vinyl Chemie) which is an emulsion in water. The resultant lacquer solution was applied to a polyester carrier film at a dry coating weight of 1.7 gsm using a drying temperature of ROC, A coherent continuous stratum of aluminum metal was then vapour deposited by standard methods upon this lacquer surface.
A layer of an aqueous based styrene butadiene adhesive was applied to the metal layer at a dry coating weight of 4 gsm to bond the substrate (Hescolina base paper 60 gsm which had been subJected to steam at 20 psi for 10 seconds) to the composite.
After 7 days the carrier film was stripped from the composite structure to produce a laminar product.
Th~n as example 3.
Mirror reflectivity 4.
The label removal time was 150 seconds.
Example 13 A lacquer solution was prepared by dissolving 80 parts by weight of Neocryl B 811 and 20 parts by weight of VinnoI H 40/55 in 210 parts by weight of butanone-2 and 90 parts by weight of ethyl acetate. To this solution was added 5 parts by weight of polyvinylàlcohol Poval *
105 ex Kuraray* dissolved in 25 parts of water.
The resultant lacquer solution was applied to a polyester carrier film at a dry coating weight of 1.7 gsm using a drying temperature of 80C.
A coherent continuous stratum of aluminum metal was then vapour deposited by standard methods upon this lacquer surface.
A layer of an aqueous based styrene butadiene adhesive was applied to the metaI layer at a dry coating weight of 4 gsm to bond the substrate (~lescoline base paper 60 gsm which had been subJected to steam at 20 psi for 10 seconds) to the composite.
After 7 days the carrier film was stripped from the composite structure to produce a laminar product.
.
~ *Trade mark .
~17~307 Then as example 3.
The resultant laminar product had a mirror reflectivity of 5 and the label released from the bottle after 160 seconds.
Example 14 A lacquer solution was prepared by dissolving 80 parts by weight of Neocryl B 811 and ~0 parts by weight of Vinnol H 40/55 in 210 parts by weight-of butanone-2 and 90 par-ts by weight of ethyl acetate. To this solution was added 10 parts by weight of Neocryl BT21 ~ex Polyvinyl Chemie) which is an emulsion in water.
The resultant lacquer solution was applied to a polyester carrier film at a dry coating weight of 1.7 gsm using ~ drying temperature of 80C.
A coherent con-tinuous stratum of aluminum metal was then vapour deposited by standard me-thods upon this la_quer surface.
A layer of an aqueous based styrene butadiene adhesive was applied to the metal layer at a dry coa-ting weight of 4 gsm to bond the substrate (Hescolina base paper 60 gsm, that had not been subJected to a steam treatment) to the composite.
After 7 days the carrier film was stripped from the composite structure to produce a laminar product~
The as example 3.
The product had a reflectivity of 6 and the label released from the bottle after 160 seconds.
:~
:
Claims (4)
1. A metallized label for containers including bottles which comprises a coating of lacquer, containing 2 to 10% by weight of an additive, wherein said percentage is calculated on the amount of resin in the lacquer and wherein said additive is soluble in an aqueous caustic soda solution containing 1.5% by weight of caustic soda, heated at 80°C.;
a stratum of metal deposited upon the lacquer coating, wherein said lacquer does not attach the metal stratum of said label; a laminating adhesive; a stratum of paper and an adhesive.
a stratum of metal deposited upon the lacquer coating, wherein said lacquer does not attach the metal stratum of said label; a laminating adhesive; a stratum of paper and an adhesive.
2. The label according to claim 1 wherein said additive has a particle size of up to 2µm.
3. The label according to claim 1 wherein said additive does not react with caustic soda.
4. The label according to claim 1 wherein said additive is selected from the group consisting of sucrose, mannitol, urea, and water based resins.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA000381815A CA1175307A (en) | 1981-07-15 | 1981-07-15 | Metallised labels |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA000381815A CA1175307A (en) | 1981-07-15 | 1981-07-15 | Metallised labels |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1175307A true CA1175307A (en) | 1984-10-02 |
Family
ID=4120446
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000381815A Expired CA1175307A (en) | 1981-07-15 | 1981-07-15 | Metallised labels |
Country Status (1)
Country | Link |
---|---|
CA (1) | CA1175307A (en) |
-
1981
- 1981-07-15 CA CA000381815A patent/CA1175307A/en not_active Expired
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